HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376087Generated: October 26, 2026
Water → 6-[5-(4-Bromo-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amide
https://huagongshe.com/reaction/1376087
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 6-Hydrazinylpyridine-3-sulfonamide | HCID 12096590 | — |
| Reactant | N-(1-ethoxy-ethylidene)-4-bromo-benzamide | HCID 21894671 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-[5-(4-Bromo-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amide | HCID 10216060 | 53% |
Reaction Steps
N-(1-ethoxy-ethylidene)-4-bromo-benzamide 565 mg (2.09 mmol) was dissolved in a mixed solvent of dichloromethane 20 ml and methanol 10 ml, and 6-hydrazinopyridine-3-sulfonic acid amide 433 mg (2.23 mmol) was added to the solution and stirred for 8 hours. After completing the reaction, water 20 ml was added to the reacting solution and extracted two times with dichloromethane, and then, the collected organic layer was washed with saturated brine. The organic layer was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure, and the resulting product was re-crystallized in acetone and hexane phase. As a result, 6-[5-(4-bromo-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amide (437 mg, yield: 53%) was obtained as a solid phase.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07169929B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-37e1e3c672ff4e11a79cc07989bc6923 |
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| Source note | uspto-grants-2007_01 |
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